Abstract
DNA barcoding is a technique for discriminating and identifying species using short, variable, and standardized DNA regions. Here, we tested for the first time the performance of plastid and nuclear regions as DNA barcodes in Passiflora. This genus is a largely variable, with more than 900 species of high ecological, commercial, and ornamental importance. We analyzed 1034 accessions of 222 species representing the four subgenera of Passiflora and evaluated the effectiveness of five plastid regions and three nuclear datasets currently employed as DNA barcodes in plants using barcoding gap, applied similarity-, and tree-based methods. The plastid regions were able to identify less than 45% of species, whereas the nuclear datasets were efficient for more than 50% using “best match” and “best close match” methods of TaxonDNA software. All subgenera presented higher interspecific pairwise distances and did not fully overlap with the intraspecific distance, and similarity-based methods showed better results than tree-based methods. The nuclear ribosomal internal transcribed spacer 1 (ITS1) region presented a higher discrimination power than the other datasets and also showed other desirable characteristics as a DNA barcode for this genus. Therefore, we suggest that this region should be used as a starting point to identify Passiflora species.
Highlights
DNA barcoding is a method that involves species identification and discrimination using short, variable, and standardized DNA regions [1,2]
The results for analyses of rbcL, matK, trnH-psbA, and the trnL (UAA) intron showed that these markers present low interspecific variability in Passiflora (Supplementary Table S1)
Our results show that internal transcribed spacer 1 (ITS1) and ITS2 presents all the desired characteristics of a DNA barcode in Passiflora, such as the highest rate of discrimination and fulfillment of amplification and sequencing requirements
Summary
DNA barcoding is a method that involves species identification and discrimination using short, variable, and standardized DNA regions [1,2]. Many different plastid loci and combinations of these loci have been proposed as promising DNA barcoding in plants [3,8]. In studies comparing different markers, some observed that each group presents distinct plastid loci or combinations of loci as an ideal barcode [9,10,11,12], whereas others highlight the challenges with the use of plastid data for some groups [13,14,15]. Many researchers have accepted that multiple markers may be necessary to obtain appropriate species discrimination [16,17]
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